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CBP/p300 and muscle differentiation: No HAT, no muscle

  • A. Polesskaya
  • , I. Naguibneva
  • , L. Fritsch
  • , A. Duquet
  • , S. Ait-Si-Ali
  • , P. Robin
  • , A. Vervisch
  • , L. L. Pritchard
  • , P. Cole
  • , A. Harel-Bellan
  • CNRS UPR 9079 Oncogénèse, Différenciation et Transduction du Signal
  • Institut André Lwoff
  • Johns Hopkins University School of Medicine

Research output: Contribution to journalArticlepeer-review

Abstract

Terminal differentiation of muscle cells follows a precisely orchestrated program of transcriptional regulatory events at the promoters of both muscle-specific and ubiquitous genes. Two distinct families of transcriptional co-activators, GCN5/PCAF and CREB-binding protein (CBP)/p300, are crucial to this process. While both possess histone acetyl-transferase (HAT) activity, previous studies have failed to identify a requirement for CBP/p300 HAT function in myogenic differentiation. We have addressed this issue directly using a chemical inhibitor of CBP/p300 in addition to a negative transdominant mutant. Our results clearly demonstrate that CBP/p300 HAT activity is critical for myogenic terminal differentiation. Furthermore, this requirement is restricted to a subset of events in the differentiation program: cell fusion and specific gene expression. These data help to define the requirements for enzymatic function of distinct coactivators at different stages of the muscle cell differentiation program.

Original languageEnglish
Pages (from-to)6816-6825
Number of pages10
JournalEMBO Journal
Volume20
Issue number23
DOIs
Publication statusPublished - 3 Dec 2001
Externally publishedYes

Keywords

  • CREB-binding protein (CBp)
  • Histone acetyl-transferase
  • MyoD
  • Myogenesis
  • p300

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